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Physical Review Letters

Saturated Optical Absorption by Slow Molecules in Hollow-Core Photonic Band-Gap Fibers

Jan Hald, Jan Conrad Petersen, J. O. Henningsen

Published May 25, 2007• 58 citations
Publisher

Abstract

We report on saturated absorption in a hollow-core photonic band-gap fiber filled with 12C2H2 molecules. We find that slow molecules provide a major contribution to the signal in the limit of low optical power and low pressure where the signal deviates significantly from the usual Lorentzian line shape. In particular, we observe a linewidth reduction of about 3 times as compared to the transit-time limited linewidth.

DOI
10.1103/physrevlett.98.213902

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We report on saturated absorption in a hollow-core photonic band-gap fiber filled with 12C2H2 molecules. We find that slow molecules provide a major contribution to the signal in the limit of low optical power and low pressure where the signal deviates significantly from the usual Lorentzian line shape. In particular, we observe a linewidth reduction of about 3 times as compared to the transit-time limited linewidth.
We investigate resonant nonlinear optical interactions and demonstrate induced transparency in acetylene molecules in a hollow-core photonic-band-gap fiber at 1.5 mum. The induced spectral transmission window is used to demonstrate slow-light effects, and we show that the observed broadening of the spectral features is due to collisions of the molecules with the inner walls of the fiber core. Our results illustrate that such fibers can be used to facilitate strong coherent light-matter interactions even when the optical response of the individual molecules is weak.
We report detailed experimental results on the optical nutation effect in acetylene-filled hollow-core photonic crystal fibers (HC-PCFs). This coherent quantum optical effect is manifested by the appearance of attenuated oscillations in the profiles of transmitted step-like coherent optical pulses. The experiments used 15 ns optical pulses with peak powers up to ∼4 W and centered at 1530.37 nm, which corresponds to the acetylene (12C2H2) vibration-rotation resonance absorption line P9. The all-fiber cell made from a HC-PCF with internal diameter ∼10.3 μm contained a gas pressure of about 0.12 Torr. The Maxwell-Bloch equations are used to analyze the influence of the homogeneous relaxation, the inhomogeneous Doppler broadening of the absorption line, and the random orientation of the acetylene molecules. By comparing the experimental results with numerical simulations, we obtain the longitudinal and the transverse relaxation times to be close to 10 ns and find that the transition dipole moment of the acetylene P9 absorption line is ∼1.36×10−32 Cm.
We perform coherent three-level spectroscopy and demonstrate induced transparency in acetylene molecules in a hollow-core photonic band-gap fiber (HC-PBF) at 1.5mu\\mumum. The induced spectral transmission window is used to demonstrate slow-light effects, and we show that the observed broadening of the spectral features is due to collisions of the molecules with the inner walls of the fiber core. Our results illustrate that such fibers can be used to facilitate strong coherent light-matter interactions even when the optical response of the individual molecules is weak.
The delayed optical nutation effect has been used to evaluate the longitudinal relaxation time (T1) inside an acetylene-filled hollow-core photonic crystal fiber (HC-PCF) at room temperature. In this experiment, sequences of two short optical pulses of 30 ns and 15 ns in width, respectively, with the maximum peak power up to ∼2.5 W, were generated at a laser wavelength of 1530.37 nm, which corresponds to the acetylene ro-vibrational P9 absorption line. The gas pressure inside the 1 m-long HC-PCF varied in the range 0.1–1 Torr. Numerical simulations based on the optical Bloch equations allowed us to evaluate the longitudinal relaxation time as T1∼9ns, proving to be fundamentally limited by the transit-time broadening. Also, the obtained results revealed the influence of slow and fast molecules in the form of a non-exponential decay of the delayed-nutation signals.
Experimental results on the transient optical nutation effect inside an acetylene-filled hollow-core photonic crystal fiber (HC-PCF) are reported. The experiments used 15 ns optical pulses with peak powers up to 5 W. The light wavelength was centered at 1530.37 nm, which corresponds to the P9 acetylene (12C2H2) vibrational-rotational absorption line. The gas pressure inside the PCF, with hollow core diameter of ∼10.3 μm, was kept around 0.12 Torr. Comparison of the experimental data with numerical simulations using the Maxwell-Bloch equations allowed us to evaluate the characteristic longitudinal and transverse relaxation times around 10 ns, as well as the transition dipole moment (1.36 × 10−32 Cm).